NDC 71335-3067 – Amlodipine Besylate and Benazepril Hydrochloride
Amlodipine Besylate 10 mg/1; Benazepril Hydrochloride 40 mg/1 · Capsule · Oral
Product NDC71335-3067
Product details
- Brand name
- Amlodipine Besylate and Benazepril Hydrochloride
- Generic name
- Amlodipine Besylate and Benazepril Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078466
- Marketed since
- October 4, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 10 mg/1
- Benazepril Hydrochloride 40 mg/1
Uses, dosage, side effects and warnings for Amlodipine Besylate and Benazepril Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3067-1 | 30 CAPSULE in 1 BOTTLE (71335-3067-1) | Feb 6, 2026 |
| 71335-3067-2 | 60 CAPSULE in 1 BOTTLE (71335-3067-2) | Feb 6, 2026 |
| 71335-3067-3 | 90 CAPSULE in 1 BOTTLE (71335-3067-3) | Feb 6, 2026 |
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